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Centaurea urvillei

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fce201bc7a456889273
Scientific name Centaurea urvillei
Authority DC.
First published in Prodr. 6: 592 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Centaurea urvillei var. leptacantha Bornm. Beih. Bot. Centralbl. 38(2): 464 (1921)

Common names Top

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Language Common/alternative name
Arabic قنطريون أورفيلي

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Centaurea raphanina subsp. raphanina Sm.
Centaurea urvillei subsp. armata Wagenitz Willdenowia 6(3): 491 (1972)
Centaurea urvillei subsp. deinacantha (Boiss. & Hausskn.) Wagenitz Fl. Iranica 139B: 388. 1980 (1980)
Centaurea urvillei subsp. hayekiana Wagenitz Willdenowia 6(3): 492 (1972)
Centaurea urvillei subsp. nimrodis (Boiss. & Hausskn.) Wagenitz Willdenowia 6(3): 494 (1972)
Centaurea urvillei subsp. urvillei DC.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Western Asia
      • East Aegean Islands
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000078581
Tropicos 2717319
KEW urn:lsid:ipni.org:names:191843-1
The Plant List gcc-35176
Open Tree Of Life 7613492
Observations.org 149261
IPNI 191843-1
iNaturalist 521604
GBIF 3128333

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Phenolic Glycosides with antiproteasomal activity from Centaurea urvillei DC. subsp. urvillei. Gülcemal D, Alankuş-Çalışkan O, Karaalp C, Ors AU, Ballar P, Bedir E Carbohydr Res 22-Nov-2010
doi:10.1016/J.CARRES.2010.09.002
PMID:20937505
Bioactivity of two Turkish endemic Centaurea species, and their major constituents Mohammad Shoeb, Stephen M. MacManus, Marcel Jaspars, Paul Kong-Thoo-Lin, Lutfun Nahar, Sezgin Celik, Satyajit D. Sarker Springer Science and Business Media LLC 29-Sep-2007
doi:10.1590/S0102-695X2007000200003
Cytotoxic Flavones From Centaurea urvillei Ayhan Ulubelen, Sevil Öksüz American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50021A025

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds / Lignan glycosides
Arctiin 100528 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1590/S0102-695X2007000200003
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1590/S0102-695X2007000200003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
2-[3-Hydroxy-5-(2-hydroxyethyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 72785824 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)CCO 316.30 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Grevilloside G 11290035 Click to see C1=C(C=C(C=C1O)OC2C(C(C(C(O2)CO)O)O)O)CCO 316.30 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP50021A025
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
https://doi.org/10.1021/NP50021A025
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
https://doi.org/10.1021/NP50021A025
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-7-yl]oxy]oxane-2-carboxylic acid 15540754 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC=C(C=C4)O 448.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3,5,6-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 49858052 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5318059 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
(2S,3S,4S,5R,6S)-Methyl 3,4,5-trihydroxy-6-((5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl)oxy)tetrahydro-2H-pyran-2-carboxylate 13844658 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 460.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
(2S)-eriodictoyl-7-O-beta-D-glucopyranosiduronic acid 10412099 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC(=C(C=C4)O)O 464.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
3,4,5-Trihydroxy-6-[3,5,6-trihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 75307446 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O)O)O 478.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 17981428 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 476.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
6-[[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxo-2,3-dihydrochromen-7-yl]oxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 3262723 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC(=C(C=C4)O)O 464.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Apigenin 7-O-methylglucuronide 5387369 Click to see COC(=O)C1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)O)O)O 460.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Hispidulin 7-O-beta-D-methylglucuronopyranoside 15219280 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O 490.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Methyl 3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-6-methoxy-4-oxochromen-7-yl]oxyoxane-2-carboxylate 74977859 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)C(=O)OC)O)O)O 490.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Naringenin 7-O-beta-D-glucuronide 71772041 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)C(=O)O)O)O)O)C4=CC=C(C=C4)O 448.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-hydroxyphenyl)-6-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13940617 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
https://doi.org/10.1021/NP50021A025
Homoplantaginin 5318083 Click to see COC1=C(C=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/J.CARRES.2010.09.002
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/NP50021A025
Hispidulin 5281628 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1021/NP50021A025
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1021/NP50021A025
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/NP50021A025
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown https://doi.org/10.1021/NP50021A025
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1021/NP50021A025

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